CanVaS: Documenting the genetic variation spectrum of Greek cancer patients-Reference-Cited by-同舟云学术

CanVaS: Documenting the genetic variation spectrum of Greek cancer patients

Published:2021-07-06 Issue:9 Volume:42 Page:1081-1093
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Human Mutation

Author:

Kalfakakou Despoina¹²^ORCID,Fostira Florentia²^ORCID,Papathanasiou Athanasios²^ORCID,Apostolou Paraskevi²^ORCID,Dellatola Vasiliki²^ORCID,Gavra Ioanna E.²^ORCID,Vlachos Ioannis S.³⁴^ORCID,Scouras Zacharias G.¹^ORCID,Drosopoulou Eleni¹^ORCID,Yannoukakos Drakoulis²^ORCID,Konstantopoulou Irene²^ORCID

Affiliation:

1. Department of Genetics, Development & Molecular Biology, School of Biology Aristotle University of Thessaloniki Thessaloniki Greece

2. Molecular Diagnostics Laboratory, Institute of Nuclear & Radiological Sciences and Technology, Energy & Safety National Center for Scientific Research “Demokritos” Athens Greece

3. Department of Pathology, Cancer Research Institute Beth Israel Deaconess Medical Center/Harvard Medical School Boston Massachusetts USA

4. Broad Institute of MIT and Harvard Cambridge Massachusetts USA

Funder

Stavros Niarchos Foundation

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/humu.24249

Reference43 articles.

1. G1738R is a BRCA1 founder mutation in Greek breast/ovarian cancer patients: evaluation of its pathogenicity and inferences on its genealogical history

2. BRCA1 and BRCA2 germline testing in Cretan isolates reveals novel and strong founder effects

3. Haplotype analysis reveals that the recurrent BRCA1 deletion of exons 23 and 24 is a Greek founder mutation

4. Diversity and inclusion in genomic research: why the uneven progress?

5. The NHGRI-EBI GWAS Catalog of published genome-wide association studies, targeted arrays and summary statistics 2019

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